ENST00000265104.5:c.9815G>T
MANE Select
|
ENSP00000265104.4:p.Ser3272Ile
|
|
ENST00000681290.1:c.9770G>T
|
ENSP00000505288.1:p.Ser3257Ile
|
|
ENST00000265104.4:c.9815G>T
|
ENSP00000265104.4:p.Ser3272Ile
|
|
ENST00000504001.3:n.527G>T
|
|
|
NM_001369.2:c.9815G>T
|
NP_001360.1:p.Ser3272Ile
|
|
XM_005248262.2:c.9770G>T
|
XP_005248319.1:p.Ser3257Ile
|
|
XM_005248262.3:c.9923G>T
|
XP_005248319.2:p.Ser3308Ile
|
|
XM_017009177.1:c.9923G>T
|
XP_016864666.1:p.Ser3308Ile
|
|
XM_017009178.1:c.8828G>T
|
XP_016864667.1:p.Ser2943Ile
|
|
XM_017009179.2:c.8828G>T
|
XP_016864668.1:p.Ser2943Ile
|
|
XM_017009180.1:c.9923G>T
|
XP_016864669.1:p.Ser3308Ile
|
|
XM_017009181.1:c.9923G>T
|
XP_016864670.1:p.Ser3308Ile
|
|
XM_017009182.1:c.9923G>T
|
XP_016864671.1:p.Ser3308Ile
|
|
XM_017009185.1:c.5012G>T
|
XP_016864674.1:p.Ser1671Ile
|
|
XM_017009186.1:c.4565G>T
|
XP_016864675.1:p.Ser1522Ile
|
|
XM_017009188.1:c.3902G>T
|
XP_016864677.1:p.Ser1301Ile
|
|
XM_024454388.1:c.8828G>T
|
XP_024310156.1:p.Ser2943Ile
|
|
XM_024454389.1:c.8417G>T
|
XP_024310157.1:p.Ser2806Ile
|
|
NM_001369.3:c.9815G>T
MANE Select
|
NP_001360.1:p.Ser3272Ile
|
|